Canonical Allele Identifier: CA414522596

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579834C>A (hg19) ; chrX:g.149498303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498303C>A , CM000685.2:g.149498303C>A	GRCh38
NC_000023.10:g.148579834C>A , CM000685.1:g.148579834C>A	GRCh37
NC_000023.9:g.148387739C>A	NCBI36
NG_011900.3:g.12032G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.512G>T MANE Select	ENSP00000339801.6:p.Cys171Phe
ENST00000651111.1:c.-122G>T	ENSP00000498395.1:n.-122G>T
ENST00000340855.10:c.512G>T	ENSP00000339801.6:p.Cys171Phe
ENST00000370441.8:c.512G>T	ENSP00000359470.4:p.Cys171Phe
ENST00000422081.6:c.-122G>T	ENSP00000477056.1:n.-122G>T
ENST00000441880.1:n.114-11205G>T
ENST00000464251.5:c.438G>T	ENSP00000428980.1:n.438G>T
ENST00000466323.5:c.512G>T	ENSP00000418264.1:p.Cys171Phe
ENST00000490775.5:n.297G>T
ENST00000523759.5:n.626G>T
NM_000202.6:c.512G>T	NP_000193.1:p.Cys171Phe
NM_001166550.2:c.242G>T	NP_001160022.1:p.Cys81Phe
NM_006123.4:c.512G>T	NP_006114.1:p.Cys171Phe
NR_104128.1:n.729G>T
NM_000202.7:c.512G>T	NP_000193.1:p.Cys171Phe
NM_001166550.3:c.242G>T	NP_001160022.1:p.Cys81Phe
NM_000202.8:c.512G>T MANE Select	NP_000193.1:p.Cys171Phe
NM_001166550.4:c.242G>T	NP_001160022.1:p.Cys81Phe
NM_006123.5:c.512G>T	NP_006114.1:p.Cys171Phe
NR_104128.2:n.681G>T